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Mosapride

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Identification
Molecular formula
C21H26ClNO5
CAS number
112885-42-4
IUPAC name
2,3-dihydro-1,4-benzodioxin-3-ylmethyl-[2-(2-methoxyethoxy)ethyl]ammonium;chloride
State
State

At room temperature, Mosapride chloride is in a solid state. It is usually encountered in the form of its crystalline powder.

Melting point (Celsius)
169.00
Melting point (Kelvin)
442.00
Boiling point (Celsius)
295.00
Boiling point (Kelvin)
568.00
General information
Molecular weight
421.95g/mol
Molar mass
421.9500g/mol
Density
1.2000g/cm3
Appearence

Mosapride chloride exhibits a crystalline solid form which typically appears white or off-white in color. It is usually available in its anhydrous form or as a hydrate, and its appearance can vary slightly depending on the form it takes.

Comment on solubility

Solubility of 2,3-Dihydro-1,4-benzodioxin-3-ylmethyl-[2-(2-methoxyethoxy)ethyl]ammonium;chloride

The solubility characteristics of the compound 2,3-dihydro-1,4-benzodioxin-3-ylmethyl-[2-(2-methoxyethoxy)ethyl]ammonium; chloride can be intriguing due to its complex structure. Several factors influence its solubility:

  • Polarity: The presence of various functional groups such as the benzodioxin component and the ammonium group may enhance its interaction with polar solvents, potentially increasing solubility in water.
  • Ionic Nature: As a chloride salt, its ionic nature often facilitates solubility in polar environments. This is typical for many ammonium salts.
  • Hydrophilicity: The ethoxy groups can contribute to **increased hydrophilicity**, which may also promote solubility in aqueous solutions.
  • Temperature: Solubility may vary significantly with temperature; increased temperatures generally enhance solubility for many compounds.

In summary, while predicting the solubility of this compound without specific experimental data is challenging, one could suggest that:

“The unique combination of polar functional groups and ionic characteristics may facilitate reasonable solubility in water, but empirical testing is essential for accurate determination.”

Understanding the solubility of this compound opens pathways for further research and application in various chemical contexts.

Interesting facts

About 2,3-Dihydro-1,4-benzodioxin-3-ylmethyl-[2-(2-methoxyethoxy)ethyl]ammonium;chloride

2,3-dihydro-1,4-benzodioxin-3-ylmethyl-[2-(2-methoxyethoxy)ethyl]ammonium;chloride is a fascinating compound with several intriguing aspects. Its unique structural features lend themselves to various applications in both biological and medicinal chemistry.

Key Facts:

  • Structural Complexity: This compound exhibits a benzodioxin core, which is notable for its stability and versatility. The additional ethylammonium group enhances its solubility in biological systems, making it an interesting candidate for drug development.
  • Potential Biological Activity: Compounds of this class may show significant pharmacological potential, including antimicrobial and anti-inflammatory activities. Research into such compounds could lead to the discovery of new therapeutic agents.
  • Synthesis: The synthesis of such complex molecules often involves intricate reactions, showcasing the beauty and creativity involved in synthetic organic chemistry. Methods may involve the use of various reagents and conditions to achieve the desired functional groups.
  • Applications: Due to its ammonium group, this compound may also serve as a surfactant or an interfacial agent in formulations, providing stability to emulsions, which can be advantageous in pharmaceuticals and cosmetics.

In summary, 2,3-dihydro-1,4-benzodioxin-3-ylmethyl-[2-(2-methoxyethoxy)ethyl]ammonium;chloride exemplifies how intricate chemical structures can lead to a range of potential applications in science and industry. As research advances, the multifaceted nature of this compound continues to open doors to new discoveries and innovations.

Synonyms
Ambenoxan hydrochloride
Ambenoxan HCl
UNII-DHR4YM0G6V
1617-99-8
DHR4YM0G6V
2-(3',6'-Dioxaheptyl)aminomethyl-1,4-benzodioxane hydrochloride
N-(2-(2-Methoxyethoxy)ethyl)-1,4-benzodioxan-2-methylamine hydrochloride
1,4-Benzodioxin-2-methanamine, 2,3-dihydro-N-(2-(2-methoxyethoxy)ethyl)-, hydrochloride
1,4-BENZODIOXAN-2-METHYLAMINE, N-(2-(2-METHOXYETHOXY)ETHYL)-, HYDROCHLORIDE
1,4-BENZODIOXIN-2-METHANAMINE, 2,3-DIHYDRO-N-(2-(2-METHOXYETHOXY)ETHYL)-, HYDROCHLORIDE (1:1)
1,4-Benzodioxin-2-methanamine, 2,3-dihydro-N-(2-(2-methoxyethoxy)ethyl)-, hydrochloride (9CI)
2,3-dihydro-1,4-benzodioxin-3-ylmethyl-[2-(2-methoxyethoxy)ethyl]azanium;chloride
Q27276399